Aurones and Flavonols from Coreopsis lanceolata L. Flowers and Their Anti-Oxidant, Pro-Inflammatory Inhibition Effects, and Recovery Effects on Alloxan-Induced Pancreatic Islets in Zebrafish

(1) Background: Many flavonoids have been reported to exhibit pharmacological activity; a preparatory study confirmed that Coreopsis lanceolata flowers (CLFs) contained high flavonoid structure content; (2) Methods: CLFs were extracted in aqueous methanol (MeOH:H2O = 4:1) and fractionated into acetic ester (EtOAc), normal butanol (n-BuOH), and H2O fractions. Repeated column chromatographies for two fractions led to the isolation of two aurones and two flavonols; (3) Results: Four flavonoids were identified based on a variety of spectroscopic data analyses to be leptosidin (1), leptosin (2), isoquercetin (3), and astragalin (4), respectively. This is the first report for isolation of 2–4 from CLFs. High-performance liquid chromatography (HPLC) analysis determined the content levels of compounds 1–4 in the MeOH extract to be 2.8 ± 0.3 mg/g (1), 17.9 ± 0.9 mg/g (2), 3.0 ± 0.2 mg/g (3), and 10.9 ± 0.9 mg/g (4), respectively. All isolated compounds showed radical scavenging activities and recovery activities in Caco-2, RAW264.7, PC-12, and HepG2 cells against reactive oxygen species. MeOH extract, EtOAc fraction, and 1–3 suppressed NO formation in LPS-stimulated RAW 264.7 cells and decreased iNOS and COX-2 expression. Furthermore, all compounds recovered the pancreatic islets damaged by alloxan treatment in zebrafish; (4) Conclusions: The outcome proposes 1–4 to serve as components of CLFs in standardizing anti-oxidant, pro-inflammatory inhibition, and potential anti-diabetic agents.


Introduction
Humans living in the modern era enjoy many advantages such as economical leisure, improvement of living standard, and growth of medicine. However, at the same time, these benefits have led to the birth of an aging society, increased stress, and caused many chronic diseases. In particular, human beings suffer from chronic metabolic diseases and so-called adult diseases, and diabetes is the most representative of these diseases. Diabetes mellitus is a metabolic disease caused by hyperglycemia, which affects more than 400 million people worldwide [1,2]. Diabetes is a disease with a high concentration of glucose in the blood due to a lack of insulin secretion or poor functioning [3]. These types of diabetes include type 1 and type 2 diabetes [4]. Type 1 diabetes results from the Compound 1, red amorphous powder, was given a molecular weight (MW) of 300, based on the detected molecular ion peak (MIP) [M + H] + m/z 301 in the positive FAB/MS spectrum (FAB + ). FT-IR data exhibited the absorption (cm -1 ) of hydroxy (3366), conjugated ketone (1661), and aromatic double bond (1604). Based on gHSQC spectra, the mentioned 1 H-NMR (PMR) and 13 C-NMR (CMR) data indicated that 1 was an aurone. PMR displayed the signals of three olefinic methines [δH 6.84 (coupling pattern, coupling constant in Hz), d, 8.2, H-5′; δH 7.26, dd, 8.2, 1.6, H-6′; δH 7.46, d, 1.6, H-2′) derived from a 1,2,4-trisubstituted benzene moiety; two olefinic methines (δH 6.73, d, 8.4, H-6; δH 7. 33, d, 8.4, H-5), owing to a 1,2,3,4-tetrasubstituted benzene moiety; one olefinic methine (δH 6.70, s, H-2); and one methoxy (δH 4.12, s, 8-OCH3) were observed. The above mentioned PMR indicated that 1 was an aurone with a methoxy group. CMR showed 16 carbon signals, confirming 1 to be composed of an aurone and one methoxy group (δC 61.7, 8-OCH3) including one conjugated ketone (δC 184. 6 26, 120.81, 126.42). CMR indicated 1 to be an aurone with three hydroxy and one methoxy groups. gHMBC correlation of the methoxy proton (δH 4.12) with the oxygen-substituted olefinic quaternary carbon (δC 133.94, C-8) which exhibited disclosing the methoxy to be at C-8. Consequently, 1 was identified to be 8-methoxymaritimetin (leptosidin), which was confirmed by comparing literature data [23] (Figure 1). Leptosidin was first isolated from Flemengia strobilifera in 1975 [24], and was reported to exhibit antioxidant activity [23].

Radical Scavenging Assays for Extract, Solvent Fractions, and Flavonoids 1-4 using DPPH and ABTS
The antioxidant capacities of extract (CLF), fractions (CLFE, CLFB, and CLFW), and compounds 1-4 of C. lanceolata flowers by the DPPH and ABTS assays are shown in Table  2. CLFE showed the highest scavenging capacities in DPPH and ABTS assay than other fractions. It was suggested that the CLFE mainly contained high amount of antioxidant

Radical Scavenging Assays for Extract, Solvent Fractions, and Flavonoids 1-4 Using DPPH and ABTS
The antioxidant capacities of extract (CLF), fractions (CLFE, CLFB, and CLFW), and compounds 1-4 of C. lanceolata flowers by the DPPH and ABTS assays are shown in Table 2. CLFE showed the highest scavenging capacities in DPPH and ABTS assay than other fractions. It was suggested that the CLFE mainly contained high amount of antioxidant flavonoids, such as leptosidin. Compounds 1-4 showed high radical scavenging capacities in order 1 > 3 > 2 > 4 in DPPH and ABTS radicals. A previous report showed that the radical scavenging capacities measured by DPPH and ABTS radicals depend on the numeric of hydroxy (OH) groups [26]. Leptosidin (1) showed the highest antioxidant capacity because of 3 , 4 -disubstitution of OH groups on the B-ring, forming a pyrocatechol structure, which is widely known to be the key structure with radical scavenging capacity. Compound 1 has one less sugar than others (2)(3)(4). The steric hindrance caused by sugars was reduced in compound 1. The aglycone of compound 3, quercetin, also has the OH group at 3 and 4 on the B-ring, forming a pyrocatechol structure. As shown in Table 2, the leptosidin glucoside, compound 2, and the quercetin glycoside, compound 3, showed two times higher activity than the kaempferol glycoside, compound 4.

Inhibition Effects of Compounds 1-4 on Intracellular
Oxidative Stress in PC-12, HepG2, Caco-2, and RAW264.7 Cells The reduction products of oxygen, i.e., reactive oxygen species (ROS), are produced by metabolic processes or external factors in normal cells in the body. Most of them have an unstable state that reaches a stable state by losing or gaining electrons. These properties are known to cause damage, various diseases, inflammation, and aging by causing oxidative stress (OS) in DNA and cell membranes in vivo [27,28]. For measuring ROS in cells, 2 ,7 -dichlorofluorescein (DCFH) diacetate is used as a typical substance. It can freely cross the cell membrane. When the acetate group is removed by esterase, it is deacetylated with non-fluorescent DCFH. Deacetylated DCFH is oxidized by ROS and, as a result, becomes a strong fluorescent DCF. Compounds 1-4 from CLF inhibited intracellular ROS in colon epithelial (Caco-2), macrophage (RAW 264.7), and neuronal (PC-12) cells. ROS levels in all cell lines were raised by OS (200 µM H 2 O 2 ), unlike their levels in control cells (Caco-2: 265.8%, RAW264.7: 188.2%, PC-12: 137.0%, and HepG2: 138.1%). After treating the cells with 10-µM isolated compounds, the results showed that all compounds significantly lowered stress induced by ROS. In particular, the decrease rates diversified by the cell line ( Figure 3). In Caco-2 colon epithelial cells, aurones 1 and 2 significantly lowered oxidative stresses, compounds 1-3 were effectual in RAW264.7 macrophages, and all flavonoids lowered oxidative stresses in PC-12 neuronal cells. These diverse rates also showed unambiguous structure-activity relationships. In the Caco-2 cells, aurones 1 and 2 were most effectual, indicating that the two pyrocatechol structure in the A-and B-ring decreased oxidative stresses. Aurone 2, which has an additional glucose compared with aurone 1, showed a little higher capacity than aurone 1. Additionally, flavonol 3, which has an pyrocatechol structure in the B-ring compared with flavonol 4, showed a little higher capacity than flavonol 4. In the RAW264.7 cells, aurones 1, 2, and flavonol 3, i.e., more catechol structures in the B-ring, correlated with higher recovery effects. In PC-12 and HepG2 cells, all compounds recuperated intracellular ROS to the control level, and no differences caused by disparateness in the structure were observed. Structure divergence of flavonoids have dissimilar absorption and conveyance rates in cells [29,30]. Thus, flavonoids with different substituents are thought to have different levels of access and absorption in different types of cells. In addition, the flavonoids have different antioxidant capacities depending on the position or numeric of their hydroxyl (-OH) and various other structural characteristics, such as double bond, methylation (-OCH 3 ), and number of saccharide [31,32]. In consequence, even though the aglycone compounds were the strongest radical scavenging effect, aurone 2 had a higher ability to reduce ROS in cells than 1. Thus, the ability to decrease the ROS in a particular cell depends on a combination of absorption, penetrability, and molecular antioxidant capacity [26].
showed a little higher capacity than aurone 1. Additionally, flavonol 3, which has an pyrocatechol structure in the B-ring compared with flavonol 4, showed a little higher capacity than flavonol 4. In the RAW264.7 cells, aurones 1, 2, and flavonol 3, i.e., more catechol structures in the B-ring, correlated with higher recovery effects. In PC-12 and HepG2 cells, all compounds recuperated intracellular ROS to the control level, and no differences caused by disparateness in the structure were observed. Structure divergence of flavonoids have dissimilar absorption and conveyance rates in cells [29,30]. Thus, flavonoids with different substituents are thought to have different levels of access and absorption in different types of cells. In addition, the flavonoids have different antioxidant capacities depending on the position or numeric of their hydroxyl (-OH) and various other structural characteristics, such as double bond, methylation (-OCH3), and number of saccharide [31,32]. In consequence, even though the aglycone compounds were the strongest radical scavenging effect, aurone 2 had a higher ability to reduce ROS in cells than 1. Thus, the ability to decrease the ROS in a particular cell depends on a combination of absorption, penetrability, and molecular antioxidant capacity [26].  To evaluate cytotoxicity for extract, fractions, as well as isolated compounds, an MTT assay was conducted. The results showed that extract (CLF), EtOAc fraction (CLFE), n-BuOH fraction (CLFB), and H2O fraction (CLFW) had no cytotoxicity up to 100 μg/mL in RAW 264.7 cells. Furthermore, compounds 1-4 had no cytotoxicity up to 100 μM, either (Supplementary Materials S7).

Inhibition Effects of Extract, Solvent Fractions, and Flavonoids 1-4 on NO formation in RAW 264.7 Macrophages
Stuehr and Marletta reported that nitric oxide (NO) is produced by mouse macrophage in response to bacterial lipopolysaccharide (LPS) [33]. Although the role of NO prevents the host from the invader, such as bacteria, excessive NO production is able to cause chronic inflammation [34]. Thus, the suppression effect of extract, solvent fractions, and compounds 1-4 on NO formation in RAW 264.7 induced with LPS was measured. Extract and CLFE dose-dependently showed the suppression effect on NO production ( Figure 4). Except for astragalin (4), all isolated compounds 1-3 significantly inhibited NO production. A total of 100 μM of flavonoids 1-4 showed the NO production by 32.9 ± 1.1%, 49.5 ± 0.7%, 62.4 ± 0.3%, and 125.7 ± 1.5%, respectively, compared with LPS-treated cells (100%) ( Figure 5). A distinct structure-activity relationship was observed in this case also. Aurones 1 and 2 showed higher efficacy in inhibiting NO production than flavonols 3 and 4 because of the existence of a catechol group. In addition, flavonol 3, which has a catechol  Stuehr and Marletta reported that nitric oxide (NO) is produced by mouse macrophage in response to bacterial lipopolysaccharide (LPS) [33]. Although the role of NO prevents the host from the invader, such as bacteria, excessive NO production is able to cause chronic inflammation [34]. Thus, the suppression effect of extract, solvent fractions, and compounds 1-4 on NO formation in RAW 264.7 induced with LPS was measured. Extract and CLFE dose-dependently showed the suppression effect on NO production ( Figure 4). Except for astragalin (4), all isolated compounds 1-3 significantly inhibited NO production. A total of 100 µM of flavonoids 1-4 showed the NO production by 32.9 ± 1.1%, 49.5 ± 0.7%, 62.4 ± 0.3%, and 125.7 ± 1.5%, respectively, compared with LPS-treated cells (100%) ( Figure 5). A distinct structure-activity relationship was observed in this case also. Aurones 1 and 2 showed higher efficacy in inhibiting NO production than flavonols 3 and 4 because of the existence of a catechol group. In addition, flavonol 3, which has a catechol structure in the B-ring compared with flavonol 4, showed a little higher efficacy in inhibiting NO production than flavonol 4. The pyrocatechol group was previously reported to inhibit NO production through the inhibition of LPS signaling and direct scavenging of NO [35]. structure in the B-ring compared with flavonol 4, showed a little higher efficacy in inhibiting NO production than flavonol 4. The pyrocatechol group was previously reported to inhibit NO production through the inhibition of LPS signaling and direct scavenging of NO [35].

Effects of Ethyl Acetate Fraction (CLFE), and Flavonoids 1-4 on Levels of Tumor Necrosis Factor (TNF)-α, Interleukin (IL)-1β, and Interleukin (IL)-6 in LPS-Stimulated RAW264.7 Cells
Macrophages and monocytes are representative immune cells, and they are activated by components derived from invading bacteria or cytokines secreted by other immune cells in the body to induce an effective inflammatory response. Stimulation of lipopolysaccharide (LPS) secretes inflammation-inducing cytokines, such as tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-1β from macrophages (including RAW 264.7 cells). Therefore, we assessed the inhibitory effects of CLFE (100 μg/mL) and flavonoids 1-4 (100 μM) on the LPS-induced production of TNF-α, IL-6, and IL-1β. RAW264.7 cells were incubated with CLFE and flavonoids 1-4 for 3 h and then stimulated with LPS for 24 h. Figure  6 showed that CLFE and flavonoids 1-4 significantly repressed TNF-α, IL-6, and IL-1β in RAW 264.7 cells. structure in the B-ring compared with flavonol 4, showed a little higher efficacy in inhibiting NO production than flavonol 4. The pyrocatechol group was previously reported to inhibit NO production through the inhibition of LPS signaling and direct scavenging of NO [35].

Inhibition Effects of Extract, Solvent Fractions, and Flavonoids 1-4 on Expression of iNOS and COX-2 in RAW264.7 Cells
Once inflammation occurred by inflammatory stimuli, iNOS continuously produces high levels of NO [36]. Furthermore, NO activates COX-2, which induces the release of

Protective Effects of Extract, Solvent Fractions, and Flavonoids 1-4 on Pancreatic Islets (PI) in Zebrafish treated by Alloxan
Protective activity of extract, solvent fractions, and isolated flavonoids 1-4 was assessed against alloxan-treated PI in zebrafish. Because of their physiological resemblances to mammals, zebrafish PI was used for model type 1 and 2 diabetes with alloxan (AX), a diabetogenic material that was reported to reduce β-cell mass in PIs [39][40][41]. To assess

Protective Effects of Extract, Solvent Fractions, and Flavonoids 1-4 on Pancreatic Islets (PI) in Zebrafish Treated by Alloxan
Protective activity of extract, solvent fractions, and isolated flavonoids 1-4 was assessed against alloxan-treated PI in zebrafish. Because of their physiological resemblances to mammals, zebrafish PI was used for model type 1 and 2 diabetes with alloxan (AX), a diabetogenic material that was reported to reduce β-cell mass in PIs [39][40][41]. To assess alloxan-treated PI, the size changes of the PIs and the fluorescence intensities of NBDGstained PIs using fluorescence microscope were analyzed. When the zebrafish larvae were exposed to alloxan, the PI size was reduced significantly by 47.8% (p = 0.0003) compared to the normal group ( Figure 8A). Zebrafish larvae treated with glimepiride, a positive control, revealed recovery capacity against AX-treated PI by a 99.5% (p = 0.0047) increase compared to AX-treated group. The PI sizes in the groups treated with extract (CLF), EtOAc (CLFE), n-BuOH (CLFB), and H 2 O (CLFW) fractions were increased by 70.0% (p = 0.0091), 68.4% (p = 0.0065), 69.8% (p = 0.005), and 73.2% (p = 0.0083), respectively, compared to the AX-treated group (Figure 8). All of the isolated compounds also resulted in an increase in PI size with statistical significance. Flavonoids 1-4 (F1-F4) increased the sizes of the damaged PIs by 98.7% (p = 0.0037), 89.8% (p = 0.0012), 78.0% (p = 0.0002), and 87.9% (p = 0.0011), respectively, compared to the AX-treated group ( Figure 8A). All isolated compounds in this study increased the sizes of AX-treated PIs with high levels of significance. In particular, leptosidin (1) displayed almost the same recovery effects as that of the positive control, i.e., glimepiride.  Figure 8A). All isolated compounds in this study increased the sizes of AX-treated PIs with high levels of significance. In particular, leptosidin (1) displayed almost the same recovery effects as that of the positive control, i.e., glimepiride.

Action of Diazoxide (DZ) on Alloxan-induced PIs in Zebrafish
In glucose-stimulated insulin secretion, metabolism of glucose in PIs is the key step [42]. Diazoxide (DZ), a KATP channel opener, was used to examine the involvement of pancreatic β-cell KATP channel stimulation activity. The PI size in the DZ-treated normal group was significantly smaller (70.4%, p = 0.0052) compared to the normal group. The AX group showed no significant differences compared to the AX + DZ-treated group. PI size in the 10-μg/mL glimepiride (GLM) + AX + DZ co-treatment groups was significantly lower

Action of Diazoxide (DZ) on Alloxan-Induced PIs in Zebrafish
In glucose-stimulated insulin secretion, metabolism of glucose in PIs is the key step [42]. Diazoxide (DZ), a K ATP channel opener, was used to examine the involvement of pancreatic β-cell K ATP channel stimulation activity. The PI size in the DZ-treated normal group was significantly smaller (70.4%, p = 0.0052) compared to the normal group. The AX group showed no significant differences compared to the AX + DZ-treated group. PI size in the 10-µg/mL glimepiride (GLM) + AX + DZ co-treatment groups was significantly lower (50.9%, p = 0.002) compared to the GLM + AX-treated groups. The AX + CLFW-treated groups were not significantly different after treatment with DZ, indicating that CLFW had no act as a K ATP channel opener. Furthermore, groups co-treated with 1 + AX, 2 + AX, and 4 + AX were not significantly different after treatment with DZ, indicating that compounds 1, 2, and 4 did not act as a K ATP channel opener. Moreover, the 3 + AX group showed significantly smaller PI sizes after treatment with DZ (61.6%, p = 0.0358) compared to the non-DZ group ( Figure 8B). These results indicate that compound 3 can stimulate insulin secretion by Ca 2+ influx via closure of K ATP channels in β-cells.

Plant Materials
Coreopsis lanceolata flowers were obtained at Kyung Hee University, Yongin, Korea in 2020 and identified by Professor Dae-Keun Kim, Woosuk University, Jeonju, Korea. A voucher specimen (KHU2020-0701) was reserved at the Laboratory of Natural Products Chemistry, Kyung Hee University, Yongin, Korea.

General Experimental Procedures
The materials and equipment used for the isolation and structure determination of constituents are described in a previous study [27].

Extraciton and Isolation
Preparation procedure of MeOH extracts (CLF) and solvent fractions (Frs), ethyl acetate (CLFE 194 g), n-butanol (CLFB 254 g), and H 2 O (CLFW 652 g) Frs from C. lanceolata flowers and the isolation procedures of compounds 1-4 from CLF are presented in Figure 9 and Figure S1. The physico-chemical and spectroscopic characteristics of isolated flavonoids are presented in Tables 3-5.

Plant Materials
Coreopsis lanceolata flowers were obtained at Kyung Hee University, Yongin, Korea in 2020 and identified by Professor Dae-Keun Kim, Woosuk University, Jeonju, Korea. A voucher specimen (KHU2020-0701) was reserved at the Laboratory of Natural Products Chemistry, Kyung Hee University, Yongin, Korea.

General Experimental Procedures
The materials and equipment used for the isolation and structure determination of constituents are described in a previous study [27].

Extraciton and Isolation
Preparation procedure of MeOH extracts (CLF) and solvent fractions (Frs), ethyl acetate (CLFE 194 g), n-butanol (CLFB 254 g), and H2O (CLFW 652 g) Frs from C. lanceolata flowers and the isolation procedures of compounds 1-4 from CLF are presented in Figure  9 and S1. The physico-chemical and spectroscopic characteristics of isolated flavonoids are presented in Tables 3-5.

Quantitative Analysis of Flavonoids 1-4 Using HPLC
The materials, equipment, and methods used for quantitative analysis of the isolated flavonoids from CLF are described in Supplementary Material S6. The solvent elution was graded as Table 6 and Table S6. The quantitative analysis was repeated three times. The materials, equipment, and methods used for the free radical scavenging assay of extract (CLF), fractions (CLFE, CLFB, and CLFW), and flavonoids 1-4 from C. lanceolata flowers are described in Supplementary Material S8 and previous studies [27,43,44].

Cell Culture and Cytotoxicity Assessment
The materials, equipment, and methods used for the cell culture and cytotoxicity assessment of extract (CLF), fractions (CLFE, CLFB, and CLFW), and flavonoids 1-4 from C. lanceolata flowers are described in Supplementary Material S8 and previous studies [27,45].

Measurement of Intracellular Oxidative Stress
The materials, equipment, and methods used for the measurement of intracellular oxidative stress of flavonoids 1-4 from C. lanceolata flowers are described in Supplementary Material S8 and previous studies [27,46].
3.6. Pro-Inflammatory Inhibition Activities 3.6.1. Determination of NO Production NO produced by RAW 264.7 cells was determined using a method described in Supplementary Material S8 and the literature [27,47].
3.6.2. Assays for IL-1β, IL-6, and TNF-α The materials, equipment, and methods used for the assays for IL-1β, IL-6, and TNF-α of ethyl acetate fraction (CLFE), as well as the flavonoids 1-4 from C. lanceolata flowers, are described in Supplementary Material S8 and a previous study [47].

Western Blot Analysis for Protein Expression
The materials, equipment, and methods used for the western blot analysis for protein expression of extract (CLF), fractions (CLFE, CLFB, and CLFW), and flavonoids 1-4 from C. lanceolata flowers are described in Supplementary Material S8 and previous studies [27,47].

Chemicals and Animals
The chemical materials used for the antidiabetic activity are described in Supplementary Material S8 and previous studies [48][49][50].

Animals
The animal preparation used for the antidiabetic activity are also described in Supplementary Material S8 and previous studies [48][49][50].

Ethics Statement
All zebrafish experimental procedures were carried out in accordance with standard zebrafish protocols and were approved by the Animal Care and Use Committee of Kyung Hee University [KHUASP(SE)-15-10].

Evaluation of Recovery Efficacy on Pancreatic Islet Damaged by Alloxan in Zebrafish
The materials, equipment, and methods used for evaluation of recovery efficacy of extract (CLF), fractions (CLFE, CLFB, and CLFW), and flavonoids 1-4 from C. lanceolata flowers on pancreatic islet damaged by alloxan in zebrafish are described in Supplementary Material S8 and a previous study [48][49][50].

Action of Diazoxide on Alloxan-Induced Diabetic Zebrafish
The materials, equipment, and methods used for action of diazoxide on alloxaninduced diabetic zebrafish are described in supplementary material S8 and previous studies [48][49][50].

Statistical Anlaysis
Results (mean ± SD, n = 3) were assessed using one-way analysis of variance and the Tukey-Kramer honestly significant difference (HSD) test, whereby p < 0.05 was considered to represent statistical significance. All statistical analyses were performed using SPSS 22.0 (SPSS Inc., Chicago, IL, USA).

Conclusions
We carried out this research to find other pharmacological active compounds from C. lanceolata flowers. Two aurones and two flavonol glucosides were isolated through repeated column chromatography using silica gel (SiO 2 ), octadecyl SiO 2 (ODS), and Sephadex LH-20 resins, and were identified by analysis of UV, IR, NMR, and MS data. Leptosidin (1) exhibited high DPPH and ABTS radical scavenging activity. All four flavonoids showed powerful antioxidation by reducing oxidative stress in intestinal epithelial cells (Caco-2), macrophage cells (RAW264.7), neuron cells (PC-12), and hepatic cells (HepG2). Extract, EtOAc fraction, and flavonoids 1-3 inhibited NO production and extract, EtOAc, n-BuOH, H 2 O fractions, and flavonoids 1-3 suppressed iNOS protein expression in RAW 264.7 cells treated with LPS. Additionally, EtOAc, n-BuOH, H 2 O fractions, and flavonoids 1 and 3 decreased COX-2 protein expression. Extract, EtOAc fraction, and flavonoids 1 and 3 were notably capable of inhibiting the pro-inflammatroy cytokines (TNF-α, IL-1β, and IL-6). Furthermore, H 2 O fraction and all flavonoids 1-4 recovered the alloxan-treated PI in zebrafish with high levels of significance. In particular, isoquercetin (3) stimulated insulin secretion by a Ca 2+ influx via closure of K ATP channels in pancreatic β-cells. The data indicate that the fractions and compounds from C. lanceolata flowers can activate the potential antioxidant effect, immune response by inhibiting excessive inflammation, and a recovery effect on damaged pancreatic β-cells. These results indicate that C. lanceolata flowers and its isolated flavonoids are used as potential anti-oxidant, pro-inflammatory inhibition, and anti-diabetic agents.
Supplementary Materials: The following are available online, The isolation procedure methods (S1), 1 H-NMR and 13 C-NMR of compounds 1-4 (S2~S5), the materials, equipment, and methods used for quantitative analysis of the isolated flavonoids from Coreopsis lanceolata flowers (S6), cell viability test of extracts, fractions, and compounds 1-4 (S7), and the methods and materials of antioxidant, pro-inflammatory inhibition, and anti-diabetic assay (S8) are available as supplementary materials.